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Canadian Left Atrial Appendage Closure Study — CLASS  

Non-Valvular Atrial Fibrillation Clinical Trial

Official title:
CLASS Canadian Left Atrial Appendage Closure Study

Clinical Trial Summary

The purpose of the study is to demonstrate the safety and the rate of closure of the Ultrasept Left Atrial Appendage (LAA) Closure System for the percutaneous occlusion of the left atrial appendage in patients with non-valvular atrial fibrillation.

Clinical Trial Description

The CLASS study is a multicenter, prospective, single arm trial designed to demonstrate the feasibility and short term efficacy of the Ultrasept Left Atrial Appendage Closure Device. Patients who present or are referred for participation in the study will be evaluated against the inclusion and exclusion criteria. Those meeting the criteria will be given the opportunity to participate. All patients will have protocol-required evaluations at each scheduled follow-up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03133806
Study type Interventional
Source Cardia Inc.
Contact Vice President of Operations
Phone 651-691-4100
Email cardia@cardia.com
Status Recruiting
Phase N/A
Start date February 15, 2017
Completion date August 15, 2018
View Details
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